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首页> 外文期刊>Journal of Biotechnology >Expression and purification of a human, soluble Arylsulfatase A for Metachromatic Leukodystrophy enzyme replacement therapy
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Expression and purification of a human, soluble Arylsulfatase A for Metachromatic Leukodystrophy enzyme replacement therapy

机译:人可溶性芳基硫酸酯酶A的表达和纯化,用于异染色质白细胞营养素酶替代疗法

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摘要

The production of active Arylsulfatase A is a key step in the development of enzyme replacement therapy for Metachromatic Leukodystrophy. To obtain large amounts of purified Arylsulfatase A for therapeutic use, we combined a retroviral expression system with a versatile and rapid purification protocol that can easily and reliably be adapted to high-throughput applications. The purification method consists of an initial ion-exchange DEAE-cellulose chromatography step followed by immuno-affinity purification using a polyclonal antibody against a 29-mer peptide of the Arylsulfatase A sequence. Immuno-adsorbed protein was eluted with a combination of acidic pH and an optimal concentration of the 29-mer peptide. This protocol reproducibly yielded approximately 100 microg of >99% pure human Arylsulfatase A, corresponding to 152 mU of enzyme activity, per liter of culture medium with properties similar to those of human non-recombinant protein.
机译:活性芳基硫酸酯酶A的生产是开发用于异色性白细胞营养不良的酶替代疗法的关键步骤。为了获得大量纯化的芳基硫酸酯酶A用于治疗,我们将逆转录病毒表达系统与通用且快速的纯化方案相结合,可以轻松,可靠地适应高通量应用。纯化方法包括一个初始的离子交换DEAE-纤维素色谱步骤,然后是使用针对芳基硫酸酯酶A序列的29-mer肽的多克隆抗体进行免疫亲和纯化。用酸性pH和最佳浓度的29-mer肽组合洗脱免疫吸附的蛋白质。该协议可重复产生每升培养基约100微克的> 99%的纯净人芳基硫酸酯酶A,相当于152 mU的酶活性,其性质与人非重组蛋白相似。

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